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Positive Processes and Transition to Health (PATH)

Primary Purpose

Major Depressive Disorder, Post Traumatic Stress Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Positive Processes and Transition to Health (PATH)
Sponsored by
Case Western Reserve University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Major Depressive Disorder focused on measuring transdiagnostic intervention, ptsd, posttraumatic stress disorder, mdd, major depressive disorder, adult, therapy, mental health, destabilizing life events, stressful life events

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Destabilizing life event involving profound loss or threat, with a minimum duration of 12 weeks since the event, but occurred within the last 5 years.
  • Between the ages of 18 and 65.
  • Elevated target: Scores of at least moderate (1 or higher) on at least 2 of the 3 target mechanisms: re- experiencing or ruminative processing of the destabilizing event (PSS-I items: 1, 2, 3, 4 or QIDS-C item 11), avoidance (PSS-I items 6, 7, 8), or reward deficits (PSS-I items 12, 13, or QIDS-C item 13).

Exclusion Criteria:

  • Current diagnosis of schizophrenia, delusional disorder, or organic mental disorder as defined by DSM-5.
  • Current diagnosis of bipolar disorder, depression with psychotic features, or depression severe enough to require immediate psychiatric treatment (i.e., serious suicide risk with intent and plan).
  • Severe self-injurious behavior or suicide attempt within the previous three months.
  • Unwilling or unable to discontinue current cognitive behavioral psychotherapy.
  • No clear memory of the destabilizing event or event occurred before age 3.
  • Unstable dose of psychotropic medications in prior 3 months.
  • Ongoing intimate relationship with the perpetrator (in assault related event).
  • Current diagnosis of a substance use disorder (DSM-5).

Sites / Locations

  • University of Delaware
  • Case Western Reserve University
  • University of Washington

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

receive PATH therapy

Arm Description

PATH includes six 60-90 min, weekly sessions, with two booster sessions for partial responders. Session 1 provides the PATH rationale and a review of life events (PATH of life: negative and positive). A rationale for an explicit focus on positive events/emotions will be provided. Sessions 2-4 focus on a verbal narrative of the destabilizing life event, reminiscence and processing of a major positive life event, and real-life practice to enact what was taught. Sessions 5 focuses on constructive processing and provides opportunity for integration and consolidation of learning. Session 6 focuses on future negative and positive events to promote application of new learning and resilience. Booster sessions focus on positive and negative life events since the last session and adaptive processes (constructive processing, approach, and reward). All sessions will include cultivation and elaboration of positive emotions to promote engagement and to build on the benefits of positive emotions.

Outcomes

Primary Outcome Measures

Affective Updating Task (Pe et al., 2013; Pe, Raes, et al., 2013)
Measure updating of affective information in working memory
Idiographic Behavioral Approach Task
Use in vivo confrontation with feared or avoided stimuli measuring avoidance behavior
Probabilistic Reward Task (Pizzagalli et al., 2005)
Assesses reward responsivity

Secondary Outcome Measures

Posttraumatic Cognitions Inventory (Foa et al., 1999)
Self-report of negative, overgeneralized stressor-related thoughts
Behavioral Activation for Depression Scale (Kanter et al., 2006)
Self-report of approach and avoidance in cognitive and behavioral domains (not specific to depression)
Snaith-Hamilton Pleasure Scale (Snaith et al., 1995)
Self-report measuring the capacity to experience pleasure

Full Information

First Posted
December 8, 2020
Last Updated
October 12, 2023
Sponsor
Case Western Reserve University
Collaborators
University of Washington, University of Delaware
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1. Study Identification

Unique Protocol Identification Number
NCT04678232
Brief Title
Positive Processes and Transition to Health
Acronym
PATH
Official Title
Treatment of Stress-Related Psychopathology: Targeting Maladaptive and Adaptive Event Processing
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Completed
Study Start Date
April 1, 2022 (Actual)
Primary Completion Date
June 30, 2023 (Actual)
Study Completion Date
June 30, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Case Western Reserve University
Collaborators
University of Washington, University of Delaware

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The R61 will be an open trial to determine if Positive Processes and Transition to Health (PATH) engages the proposed targets: unproductive processing, avoidance, and reward deficits in a sample of 45 adults who have experienced a destabilizing life event involving profound loss or threat, report persistent stressor-related symptoms of PTSD and/or depression, and are elevated on symptoms related to 2 of the 3 therapeutic targets. Additionally, will examine whether patients perceive PATH as helpful and complete/adhere to treatment, and therapist fidelity. Patients will receive 6 sessions of PATH (with 2 boosters, if partial responders). Primary targets will be assessed at pre-treatment, week 4, post-treatment, and at 1- and 3-month follow-up; secondary targets at pre-treatment, weekly during treatment, post-treatment, and at 1- and 3-month follow-ups.
Detailed Description
Evidence-based psychotherapies for posttraumatic stress disorder (PTSD) and depression consistently produce strong, clinically meaningful effects for many individuals. However, these interventions also have significant dropout rates, a large minority of individuals continue to have debilitating symptoms, and even those who respond may be vulnerable to relapse upon future stressors. More efficient and mechanistically precise interventions are needed. Consistent with the cross-cutting theme of studying the role of the environment in the NIMH Strategic Plan, the etiological role of exposure to destabilizing, stressful life events is common to both PTSD and depression. Not only do they share common distress-related triggers, symptoms, and maintaining processes, but they also commonly co-occur (upwards of 60%). Current PTSD and depression treatments typically focus on their respective disorders rather than on common processes that maintain psychopathology; and, importantly, they do not explicitly target positive adaptive processes associated with resilience. Decades of experimental studies, prospective studies, and psychotherapy trials have identified interconnected maladaptive and adaptive processes associated with persistent psychopathology after stressful, destabilizing events. These maladaptive processes include: 1) unproductive event processing; 2) avoidance; and 3) reward sensitivity and processing deficits. These processes prolong negative mood, interfere with adaptive coping and processing of emotional material, and increase sensitivity to future stressful life events. PATH (Positive Processes and Transition to Health) directly targets these maladaptive processes while also teaching parallel adaptive skills (constructive processing, approach, and positive emotion processing and reward seeking). Six, 90-min sessions target individuals who have experienced a destabilizing life event and have persistent stressor-related symptoms. PATH utilizes life event processing (revisiting, meaning making), focusing repeatedly on an identified destabilizing life event, positive life events, and future events as a framework to identify maladaptive processes and teach constructive processing skills. PATH has the potential to reduce dropout, improve treatment engagement and outcomes, identify potential treatment mechanisms, and ultimately reduce the costly human and economic burden of stressor-related psychopathology. For the open trial's "Go" to be achieved and to proceed to the R33, two criteria must be met. The first is that at least 2 of the 3 primary targets must change via PATH. A moderate effect size (d = 0.60) was chosen to reflect evidence of clinically meaningful target engagement (see Gold et al., 2017), in line with NIMH guidelines for a preliminary signal of target engagement/efficacy in intervention trials. Second, at least one of the secondary measures must show a moderate effect (d = 0.50) from pre- to post-treatment. We included measures of each of the targets, as they are conceptualized as interrelated parts of a "stuck" system. For "Go" to an R01 after the R33, in addition to target engagement, primary outcomes of PTSD and depression must show clinically meaningful gains (e.g., Barth et al., 2016; Cusak et al., 2016).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Major Depressive Disorder, Post Traumatic Stress Disorder
Keywords
transdiagnostic intervention, ptsd, posttraumatic stress disorder, mdd, major depressive disorder, adult, therapy, mental health, destabilizing life events, stressful life events

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
All participants will receive PATH therapy.
Masking
None (Open Label)
Allocation
N/A
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
receive PATH therapy
Arm Type
Experimental
Arm Description
PATH includes six 60-90 min, weekly sessions, with two booster sessions for partial responders. Session 1 provides the PATH rationale and a review of life events (PATH of life: negative and positive). A rationale for an explicit focus on positive events/emotions will be provided. Sessions 2-4 focus on a verbal narrative of the destabilizing life event, reminiscence and processing of a major positive life event, and real-life practice to enact what was taught. Sessions 5 focuses on constructive processing and provides opportunity for integration and consolidation of learning. Session 6 focuses on future negative and positive events to promote application of new learning and resilience. Booster sessions focus on positive and negative life events since the last session and adaptive processes (constructive processing, approach, and reward). All sessions will include cultivation and elaboration of positive emotions to promote engagement and to build on the benefits of positive emotions.
Intervention Type
Behavioral
Intervention Name(s)
Positive Processes and Transition to Health (PATH)
Other Intervention Name(s)
PATH
Intervention Description
See arm/group description for details regarding this intervention
Primary Outcome Measure Information:
Title
Affective Updating Task (Pe et al., 2013; Pe, Raes, et al., 2013)
Description
Measure updating of affective information in working memory
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)
Title
Idiographic Behavioral Approach Task
Description
Use in vivo confrontation with feared or avoided stimuli measuring avoidance behavior
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)
Title
Probabilistic Reward Task (Pizzagalli et al., 2005)
Description
Assesses reward responsivity
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)
Secondary Outcome Measure Information:
Title
Posttraumatic Cognitions Inventory (Foa et al., 1999)
Description
Self-report of negative, overgeneralized stressor-related thoughts
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)
Title
Behavioral Activation for Depression Scale (Kanter et al., 2006)
Description
Self-report of approach and avoidance in cognitive and behavioral domains (not specific to depression)
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)
Title
Snaith-Hamilton Pleasure Scale (Snaith et al., 1995)
Description
Self-report measuring the capacity to experience pleasure
Time Frame
Change from baseline score at 6 weeks (immediately post treatment)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Destabilizing life event involving profound loss or threat, with a minimum duration of 12 weeks since the event, but occurred within the last 5 years. Between the ages of 18 and 65. Elevated target: Scores of at least moderate (1 or higher) on at least 2 of the 3 target mechanisms: re- experiencing or ruminative processing of the destabilizing event (PSS-I items: 1, 2, 3, 4 or QIDS-C item 11), avoidance (PSS-I items 6, 7, 8), or reward deficits (PSS-I items 12, 13, or QIDS-C item 13). Exclusion Criteria: Current diagnosis of schizophrenia, delusional disorder, or organic mental disorder as defined by DSM-5. Current diagnosis of bipolar disorder, depression with psychotic features, or depression severe enough to require immediate psychiatric treatment (i.e., serious suicide risk with intent and plan). Severe self-injurious behavior or suicide attempt within the previous three months. Unwilling or unable to discontinue current cognitive behavioral psychotherapy. No clear memory of the destabilizing event or event occurred before age 3. Unstable dose of psychotropic medications in prior 3 months. Ongoing intimate relationship with the perpetrator (in assault related event). Current diagnosis of a substance use disorder (DSM-5).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Norah C Feeny, PhD
Organizational Affiliation
Case Western Reserve University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Delaware
City
Newark
State/Province
Delaware
ZIP/Postal Code
19716
Country
United States
Facility Name
Case Western Reserve University
City
Cleveland
State/Province
Ohio
ZIP/Postal Code
44106
Country
United States
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98195
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Positive Processes and Transition to Health

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